194 English-speaking jobs in Walloon Brabant

Internship opportunity in Vaccine Manufacturing Technology & Lyophilization. Explore bioprocessing technologies, interact with suppliers, and support freeze-drying process development. Must be enrolled in a relevant Bachelor/Master program in Europe and fluent in English.

The Student Funding Officer will communicate with enquirers, process applications, and provide information. The role requires proficiency in Microsoft Office Suite, strong communication skills, and the ability to work independently and meet deadlines.

The LMCC Engineer ensures coordination between line maintenance providers and minimizes maintenance impact on flight operations. Responsibilities include managing scheduled and unscheduled maintenance, reporting technical disruptions, and acting as a central point of contact for AOG situations.

Associate Director will lead the content approval process for vaccines within GSK.

Accounts Receivable & Collections Accountant needed for a growing Canadian subsidiary of a global manufacturing group. Responsibilities include managing accounts receivable, collections, supporting accounts payable, and assisting with month-end close.

Shape and execute the enterprise-wide Data, Analytics, AI, and Insight strategy for Supply Chain. Lead teams, elevate data governance, and ensure high-quality, compliant data. Collaborate with leaders across Global Supply Chain, Digital Technology, Quality, Finance, Procurement, Manufacturing, and other key business partners.

The Oncology Pipeline MSL is a field-based role connecting GSK to the healthcare community. This non-promotional position focuses on advancing clinical practice to improve patient outcomes. The MSL engages with healthcare providers and account personnel to ensure understanding of GSK medicines, their benefit/risk profile, and the evolving treatment landscape. Responsibilities include identifying and engaging with healthcare professionals, contributing to medical strategy by collecting and communicating medical insights, and supporting clinical trials.

Internship opportunity in Global Regulatory Affairs supporting vaccine development and lifecycle management. Tasks include preparing regulatory documents, compiling market requirements, and assisting with IT tool deployment. Must be enrolled in a relevant Master's program in Europe and proficient in English.

The Systems Performance Engineer I provides frontline technical support and troubleshooting for complex automated sterilization systems. Responsibilities include diagnosing and resolving issues across software services, databases, HMIs, and system interfaces, coordinating with internal teams, and ensuring timely communication with customers.

Field Service Engineer for Radiopharma Systems will install, maintain, and repair high-energy accelerator components at customer locations worldwide. Responsibilities include troubleshooting, training colleagues, and documenting interventions. Requires a Master's degree in electro-mechanics or equivalent, experience with complex systems, and strong communication skills. Must be willing to travel up to 60% of the time.

Provides scientific leadership for non-clinical safety across discovery and development programs. Develops and executes non-clinical safety strategies, ensures high-quality data delivery, and supports regulatory interactions.

The Systems Performance Engineer I provides technical support and troubleshooting for complex automated sterilization systems. Responsibilities include diagnosing and resolving issues across software, hardware, and system interfaces, coordinating with internal teams, and communicating with customers.

Processes invoices for German entities, ensuring proper documentation and approvals. Monitors vendor statements, investigates discrepancies, and reconciles accounts. Requires 5+ years of AP or general accounting experience and proficiency in Microsoft Office.

Leads business development and sales activities for strategic, complex services programs across EMEA, focusing on nuclear plant major component replacements, modernizations, and life-extensions.

Leads external clinical manufacturing strategy for drug substance and drug product across development stages. Manages technology transfer, batch manufacturing, and logistics with CMOs. Collaborates with cross-functional teams and regulatory stakeholders.

The CSQA Specialist ensures compliance of GxP computerized systems with regulatory requirements and industry best practices. This role provides expert guidance on CSV/CSA, data integrity, and quality oversight of digital initiatives. The CSQA Specialist collaborates with cross-functional teams to mitigate data integrity risks and drive continuous improvement.

Develop, validate, and industrialize secondary and tertiary packaging components for global packaging operations. Manage projects, change controls, and stakeholder communications. Apply packaging regulations and standards in development and manufacturing.

External Manufacturing Operations Lead for Drug Substance will oversee performance of contract manufacturing organizations (CMOs) and key suppliers. Responsibilities include ensuring reliable supply, issue resolution, and strong partnerships with stakeholders. The role requires a Master's degree or PhD in life sciences with at least 7 years of relevant experience.

RELEX Functional Consultant needed for a 12-month freelance contract to support the rollout and optimization of a RELEX forecasting and replenishment solution.

Senior Project Procurement Specialist leads procurement activities for multiple programs, ensuring readiness for pre-pilot, pilot, and execution phases. Develops sourcing plans, manages supplier relationships, and negotiates contracts for equipment and services. Collaborates with internal teams and external suppliers to achieve project goals. Requires a background in supply chain management, technical expertise, and strong communication skills.